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Idiopathic Capital Femoral Chondrolysis: A Case Report
Idiopathic capital femoral chondrolysis is a rare condition most commonly seen in African-American pre-adolescent females. The primary symptoms are hip stiffness and pain, which are accompanied by limping. Physical examinations typically reveal an external rotation contracture, flexion contracture,...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cureus
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9533635/ https://www.ncbi.nlm.nih.gov/pubmed/36225422 http://dx.doi.org/10.7759/cureus.28789 |
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author | Gupta, Pranav Gupta, Dhananjay Shrivastav, Sandeep |
author_facet | Gupta, Pranav Gupta, Dhananjay Shrivastav, Sandeep |
author_sort | Gupta, Pranav |
collection | PubMed |
description | Idiopathic capital femoral chondrolysis is a rare condition most commonly seen in African-American pre-adolescent females. The primary symptoms are hip stiffness and pain, which are accompanied by limping. Physical examinations typically reveal an external rotation contracture, flexion contracture, and abduction contracture. There is also immobility at the hip secondary to muscle spasms. Here, we present and discuss the follow-up case of a 10-year-old female patient who was diagnosed with idiopathic chondrolysis of capital femoral epiphysis, right side, and underwent right hip arthroscopic evaluation and lavage. At follow-up two months after the right hip arthroscopic evaluation, she presented with painless limping on the right side. The patient underwent soft tissue release right hip under general anaesthesia and was discharged in stable condition. |
format | Online Article Text |
id | pubmed-9533635 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Cureus |
record_format | MEDLINE/PubMed |
spelling | pubmed-95336352022-10-11 Idiopathic Capital Femoral Chondrolysis: A Case Report Gupta, Pranav Gupta, Dhananjay Shrivastav, Sandeep Cureus Pain Management Idiopathic capital femoral chondrolysis is a rare condition most commonly seen in African-American pre-adolescent females. The primary symptoms are hip stiffness and pain, which are accompanied by limping. Physical examinations typically reveal an external rotation contracture, flexion contracture, and abduction contracture. There is also immobility at the hip secondary to muscle spasms. Here, we present and discuss the follow-up case of a 10-year-old female patient who was diagnosed with idiopathic chondrolysis of capital femoral epiphysis, right side, and underwent right hip arthroscopic evaluation and lavage. At follow-up two months after the right hip arthroscopic evaluation, she presented with painless limping on the right side. The patient underwent soft tissue release right hip under general anaesthesia and was discharged in stable condition. Cureus 2022-09-05 /pmc/articles/PMC9533635/ /pubmed/36225422 http://dx.doi.org/10.7759/cureus.28789 Text en Copyright © 2022, Gupta et al. https://creativecommons.org/licenses/by/3.0/This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Pain Management Gupta, Pranav Gupta, Dhananjay Shrivastav, Sandeep Idiopathic Capital Femoral Chondrolysis: A Case Report |
title | Idiopathic Capital Femoral Chondrolysis: A Case Report |
title_full | Idiopathic Capital Femoral Chondrolysis: A Case Report |
title_fullStr | Idiopathic Capital Femoral Chondrolysis: A Case Report |
title_full_unstemmed | Idiopathic Capital Femoral Chondrolysis: A Case Report |
title_short | Idiopathic Capital Femoral Chondrolysis: A Case Report |
title_sort | idiopathic capital femoral chondrolysis: a case report |
topic | Pain Management |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9533635/ https://www.ncbi.nlm.nih.gov/pubmed/36225422 http://dx.doi.org/10.7759/cureus.28789 |
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